Showing posts with label PMDD Awareness UK. Show all posts
Showing posts with label PMDD Awareness UK. Show all posts

Tuesday, 14 July 2015

PMDD in Chat it's fate magazine.

Today, my story came out in the August edition of Chat it's fate magazine.  I was contacted by them earlier in the year to share my story about PMDD, the menstrual cycle and my art.  I felt this was a way to raise some awareness of how severe PMS can become, along with how I came to heal myself from the worst symptoms.  If you would like to read my story you can find it in all larger newsagents for the next month.

If you are interested in finding out more about PMDD, please check out my PMDD blog, Meet My PMDD, or visit the UK's National Association for Premenstrual Syndrome (NAPS) or the USA's National Association for Premenstrual Dysphoric Disorder.

To find out more about the alternative ways of understanding the menstrual cycle, please have a read through my Natural Shaman blog, particularly the article I wrote for Indie Shaman magazine, The Magic of the Menstrual Cycle and my experience at a menstrual workshop with Alexandra Pope.

Sign up to learn more about your menstrual cycle with Red School Online.  Red School Online is a new way to learn about your cycle, with peer support, fantastic learning tools and private group chat.  Go check it out!

Red School also features some of my work in their teaching materials, you can find my poster in my Etsy store.  If you would like to see more of my feminine art work, please visit my gallery over at chaoticat.com.

Friday, 3 April 2015

PMDD Awareness Month 2015

Show your support! 

The National Association for PMDD is continuing the PMDD Awareness month throughout April. 

Use the hashtag #pmddbrave


Monday, 16 June 2014

Handing things over...


Recently, I decided I can no longer maintain the PMDD-Community page and PMDD Awareness UK pages on Facebook.  It breaks my heart every time I cannot respond to a message, and the pages need an injection of energy and enthusiasm that I just can't muster now towards PMDD things.

Within a few days of the call out on the community page I had found someone perfect for the position.  It's a challenging place to be when you have thousands of likers and you can no longer continue what you started, so it was always my priority to hand over to people who I feel have every intention of keeping these spaces going to the best of their ability.  Jenn Stephan has experience in running pages and women's health, alongside being a PMDD sufferer and is looking forward to adding more content and creating conversations on the page.  I'm sure she will do just great.

So, I bid farewell to a community I have looked after for 4 years.  It is both a sad and happy time.  It will be strange not to check in on the page every couple of days and to no longer have the responsibility to reply to comments and queries.  I am looking forward to really being able to move on without thinking about PMDD or being called back to help someone else in need.  It may sound selfish, but I know I have dedicated a lot of my life to helping others while healing myself, but for this next part of the journey I need to go it alone (symbolically!).  I still run a a couple of support groups (I don't know if I might need some support during the next part of my journey, or if that's even the right place, but it feels right to still have some connections there)

The PMDD Awareness UK page is also being handed on to a lady called Victoria.  Victoria currently admins the UK support group and is looking to help raise more awareness.  Victoria's own journey with PMDD sees her recovering from a hysterectomy, so if there is anyone who can understand first hand the struggles of living with PMDD it's her.  I'm hoping she will enjoy running the page and helping others as much as I have.  Taking hold of the PMDD baton and running with it is essential to the future of PMDD being understood, so I hope these women realise they are doing a worthwhile and needed job for others with the condition.

My best wishes to them both.  The posts I make to these pages over the next few days will be my last, as I help the new ladies find their feet.  I will always remember what was achieved and how much support I got through these spaces.  If you are searching for help, go there now and ask for help.  Someone is there waiting to listen and share advice.

Much love x

Friday, 28 March 2014

PMDDAUK Closing

It is with sadness that I have to tell you that the PMDD Awareness UK website will be closing.  Other commitments and developments in my life means I can no longer maintain this website along with my other projects.

All donated stories will be re-published here over the coming weeks.  Thank you to everyone who helped, shared stories and supported this venture.  Hopefully we will see change for PMDD sufferers in the future.

I will continue to accept stories and publish them here, so feel free to get in touch if you'd like to share something via this blog.

If there is anything good about having to close down the site it's that I no longer suffer in the same way as I used to.  I have got my life back.  I am not cured or mood free, but I am persuing goals I never thought would happen, I am enjoying life, and more often happy than not.

I hope this can at least give others hope that life isn't over if you have PMDD.  Things change and no matter how awful things are, it's always worth the fight to keep going.

Thank you again to all who have supported me and PMDDAUK.  It may not have worked out, or lasted very long, but I tried.  Life changes, things move on, and all we can do is move with it.

With lots of love

Cat

To keep up with all my new projects, please visit my art website, www.chaoticat.com or Artist Facebook Page. xx


Friday, 17 May 2013

Wonderful Women's Day

I have very kindly been asked to talk about PMDD at a local Wonderful Women's Day.

The whole day is incorporating lots of activities, including an opportunity to experience Miranda Gray's Womb blessing in the company of others, AND a viewing of the film 'Things we don't talk about'.

If you live in the Hampshire area, why don't you come along!

For more details about activities please click the following links.

Miranda Gray's Womb Blessing http://www.wombblessing.com/
(You must register with Miranda to receive the womb blessing, chose 12 noon as the time if you are coming along on the day)

'Things we don't talk about' - Red Tent Movie http://www.redtentmovie.com/
(Admission to film only will be at 5.30pm with a suggested donation of £7)

Event run and organised by The Dreadess http://www.thedreadess.com/#/wonderful-womens-day/4576189163


Wednesday, 3 April 2013

Birthing Pain.

Lots of new things have happened recently.  The PMDD Community page I have been an admin of for the past two years was handed over to me with full control.  This meant that I now had the control to try and make it more active and spend a little more time on it.  I have taken on new admins and am sharing the work load over there as the priority for me is my new website and maintaining this blog.

With the launch of the new website www.pmddawareness.co.uk, amd PMDD Awareness month, I have been really busy.  Couple that with Easter holidays and work being done around the house, life has been a bit hectic.

In birthing these new projects, these new ideas, I came across some people who wanted to bring it all down.  It was a shock, and to be honest, ruined my Easter with the family.  Taking abuse on Facebook from people you've tried to help is not nice.  Being publicly slagged off when you've trusted someone is also uncalled for.  Seeing someone ripping off your ideas, using my images and then having the audacity to accuse me of things I haven't done.  I have been dealing with a ton of anxiety and stress with it all and it did almost break me.

I ended up thinking... right.. I'll go offline.  I'll throw in the towel and forget about PMDD Awareness UK.  I'll go private again.  I'll withdraw.

I started thinking about birth.  The project I've been planning for over 6 months has now just been 'birthed'.  What happens in the birth process?  There is pain.  There is doubt.  There is fear.

PMDD Awareness UK is my baby.  Someone was threatening that, making me feel like I shouldn't be doing it, that I am a bad person.  But it was about to be out there.. I had already announced it would be going live.  Can you stop labour? Can you push a baby back in?  Can you say NO, I don't want this when the head has already come out?

It's taken me days to shake the negative feelings and thoughts.  I'm in a part of my cycle when it's more difficult coping with stressful situations.  I am never gonna get this person to see what happened from my side.  It may have been a PMDD outburst, but that's no excuse for abusing privileges and getting nasty, accusing me of things I simply haven't done and getting others to get involved.

I almost took the site down.  I almost gave up.

But how can that be right?  Why should I give up on all I have done because of one person who has taken a dislike to me.  I get more messages of support and thanks than one persons hatred. 

So, no...  I'm staying put.  I DO have my limits at what I can contribute to the PMDD 'cause'  and I am pretty much there.  The next step is up to others.  I was also accused the week of being egotistical and 'wanting it all for myself'.  That is ludicrous.  To move forward with raising awareness is up to each and every sufferer and their families out there.  I've pretty much done all I can do. 

My blog will always be here for me to share with you things in my life, and the PMDD Awareness site will stay as an online presence for PMDD in the UK.  Providing links to groups, organisations, information and encouraging others to do what they can.  I still have a few things I wish to achieve with regard to PMDD in the UK but this is where I pretty much hit my limit.  Maintaining two PMDD related websites and the groups along with the other things going on in my life... other projects and life paths I wish to follow is more than enough for someone with PMDD to cope with.  I could have never imagined I would get a hold of my PMDD enough to achieve any of it, but at some point, I have to start spending my time on the things that heal me.

Thank you to all my friends who supported me through this last weekend.  I really couldn't do this without the support of you all...

Friday, 29 March 2013

New PMDD Website now LIVE!

Finally!

Six months in the creation (slow and steady wins the race) and here it is!

www.pmddawareness.co.uk

Go check it out!




Tuesday, 12 March 2013

NAPS Study Day

National Association for Pre menstrual Syndrome (NAPS)
Study Day on Women's Health - 1st March 2013

Women and their Hormones

I was very kindly invited along to the recent NAPS Study day on Women's Health in Southampton. As a PMS Lay Champion, PMDD sufferer and Health Activist I was permitted to attend the event which is usually only for medical professionals and trainee's. It was an amazing opportunity for me to get a window into what goes on behind the scenes and a perfect opportunity to share with others and let them know what happens at these things!  Thankfully, I was in the ovulatory phase of my cycle, and so was able to attend. Had the conference been held a week later, I may not have made it!

The venue (The Hub Theatre in Southampton) was very nice. Bright, clean and welcoming. It was really lovely to meet Jackie, the CEO of NAPS, as we had spoken via email quite a few times. I was a bit nervous, but after a coffee and a chat with Jackie, It felt good to be there.

Talks started with Mr Nick Panay, Consultant Gynaecologist and the Chairman of NAPS. After an introduction to the day and NAPS, he went on to talk us all through the NAPS guidelines on the management of PMS. These guidelines are available for £5 from the NAPS website and provide a very useful tool for GP's and patients when devising plans for managing PMS. Nick touched on the history of PMS, quoting Hippocrates and that the first time anyone made any connections between PMS and cyclical ovarian activity was in 1873 by Henry Maudsley. In the 19th century many called it 'Menstrual madness' and believed it was brought on by women reading serious books or playing music! By 1931 the term Pre Menstrual Tension was coined and in 1953, Dalton and Greene introduced the term Pre Menstrual Syndrome. In 1957 Katharina Dalton set up the first ever PMS clinic. The National Association of Pre menstrual Syndrome was founded by Dalton in 1983 and 5 years later, Professor John Studd discovered that menstruation was not an essential feature of PMS and began to use the term Ovarian Cycle Syndrome. Despite the recognition in the medical profession, the stereotypes, myths and taboos that surround menstruation continue to this day, with negative articles in women's magazines still being published. You would have thought that with all the research and support from medical professionals that this would no longer happen, but unfortunately PMS is still the butt of many jokes and is not taken seriously by the general population.

Mr Panay's talk was followed by Dr Carrie Sadler (GP and Associate Specialist in Reproductive health) and Ms Annie Hawkins (O+G Locum Consultant at Chelsea and Westminster Hospital) who shared results taken from the Southampton Women's Survey and the NAPS Survey 2011. It was interesting to know that such a study had taken place. The Southampton Women's Survey started in the 1990's and interviewed over 12000 non pregnant women and included questions about PMS. The survey also followed these women through pregnancy and the development of their children. The most interesting conclusion was that women were less likely to have symptoms if they had been educated about the effects of the menstrual cycle and how to manage their symptoms. It was also noted that stress was a major factor in the severity of symptoms. Both surveys showed the need for more research and funding for raising awareness.

I would like to see more education for teenage girls in schools. If we educated our daughters about the menstrual cycle and how to see the early warning signs that their menstrual cycle may be becoming troublesome, I think we could reduce the incidences of extreme PMS or PMDD. Girls learn the basic bodily functions in school, and how to deal with having a period, but who talks to them about how they might FEEL? From personal experience, many women are unaware of what a detrimental effect the menstrual cycle can have on their mental health and well being and many who suffer from PMDD feel like they are actually 'going mad' or suffering from a severe mental health problem. If these women had known that the menstrual cycle CAN cause such severe problems I think we could see more women taking more control of their own bodies and cyclical problems, maybe even 'nipping it in the bud' before PMS (which can be treated relatively easily) develops into an extreme disorder. Stress is the main enemy of women who suffer from PMS, PMDD, fertility problems and sexual problems. This point was re-iterated many times throughout all the lectures.

Next up was Dr Alain Gregoire, (Consultant Psychiatrist at Southampton) talking about giving good ante-natal and post natal care. Dr Gregoire was an entertaining animated speaker who introduced us to a variety of facts regarding the research done on the effects of depression in pregnancy and how it can affect the child later on in life. He also noted that despite the research proving that mothers pre disposed to depression were highly likely to have problems post natally, that very little was in place to support these mothers. It made me realise that the doctors and specialists are probably just as frustrated with the way things are here in the UK as the patients themselves, and that many are working hard to change things. They are limited by funding, lack of research and all the red tape that surrounds working within the medical profession.

Ms Dani Singer, Adult Psychotherapist, London talked about the psychological aspects of premature ovarian sufficiency and highlighted the need for sensitive labelling of such disorders. Using words such as failure or dysfunction can create a negative reaction in the patient and lead to a misunderstanding of the problem itself. Labels are not always helpful to the condition. I had noted that Mr Nick Panay had mentioned that PMDD was the American term for Extreme PMS, and in the UK, doctors prefer the term Extreme PMS. I know from the women I have spoken to with PMDD, that to be associated with PMS is to almost disregard how bad PMDD episodes can be. If you tell someone you have Extreme PMS, then the main thing they hear is PMS and as we know, that is rarely taken seriously, so I do feel that a distinction should be made between PMS and it's extreme form. Many women relate to the dysphoric element of the description PMDD, and I feel it should have it's own name.. after all, it is currently described in the draft for the ICD 11 as 'a distinct clinical entity'.

Diet and the Menstrual Cycle was the topic presented by Ms Amanda Moore, Nutritionist, London. This was a fantastic talk highlighting the benefits of a healthy, low GI diet and it's positive effects on pre menstrual symptoms. You can devise nutrition plans depending on the symptoms presented. If you have more physical problems, foods to help support those bodily functions may help relieve symptoms, if it's more psychological, then foods can be prescribed to help with brain health and function. I think many women could do a lot more to help fight their PMS symptoms if they were more aware of what was good and bad to eat (although the bad is obvious in most cases!) The talk made me realise that I need to start getting more oily fish in my diet! Twice a week please! It also confirmed my thoughts that people in the UK can suffer greatly from a lack of vitamin D, which in turn reduces our serotonin levels. In some cases this can develop into Seasonal Affective Disorder, which can mean women with PMS/PMDD can suffer much more during the winter months in the UK.

The debate of the day was supposed to be between Professor John Studd (Professor of Gynaecology, London PMS and Menopause Centre) and Ms Claudine Domoney (Consultant O+G, Chelsea and Westminster Hospital). The topic – HRT can be taken forever. Unfortunately, Professor Studd was unable to attend, so we were all entertained by Claudine presenting both sides of the debate with an occasional comment from Nick Panay! It was very interesting and Claudine provided some much needed light relief after an intense morning of lectures. It was concluded that the newer bio-identical forms of HRT are safe for continuous use as they work in very small doses, and if an individual is happy with their medication there is no real reason to stop. What was also enlightening was hearing the frustrations of doctors who have had certain HRT medications discontinued.. often for no other reason than profitability to the drug company. It highlighted again that the doctors really do try to do their best, but are often restricted by the price of medications and are at the mercy of the drug companies that make and supply them.

After a brief break for lunch, we were back into the theatre for a discussion on contraception with Gilly Andrews, Clinical Nurse Specialist, London. It was amazing to hear about the advances in the contraceptive pill and the different types of pill coming onto the market. It was also explained that the reasons certain brands of pill are available abroad but not in the UK are because our own health authorities refuse to allow them to be prescribed over here. This is often down to the cost of the medications, or concerns over safety. If you are considering contraception and suffer from PMS, ask your GP or Family Planning Clinic for details of the newer contraceptive pills, such as Yasmin and Qlaira, and products such as the Nuvaring.

The afternoon talks moved away from the subject of PMS. Ms Claudine Domoney and Ms Annie Hawkins looked at sexual problems in women and how to diagnose correctly by taking into account other factors such as stress and background. Mr Tim Hillard, Consultant Obstetrician and Gynaecologist from Poole Hospital discussed pelvic floor disorders and the best way to help patients, including some really effective methods of treatment and Mr Michael Dooley, Consultant Gynaecologist and Medical Director from The Poundbury Clinic talked about fertility and the menopause, including what effects fertility and ways of dealing with infertility.

The day had been fascinating. It had been a pleasure to meet Nick Panay and the people behind the scenes at NAPS. Although I am no longer going down a medical or surgical route for managing my PMDD, I am very grateful for the work that all these specialists are doing. It had been said at the start of the day, that often, the first thing a patient does when they meet a specialist who understands their condition is shed some tears. I know that feeling well. I have met only a few medical professionals in my life who have taken me seriously, who have helped me and supported me. It was their understanding and belief that helped me to come to terms with what was going on, that it WAS real and there was an explanation. It enabled me to (eventually) become strong enough to do what I am doing now, which believe me, is not what I'd had in mind!

The next step for me is the launch of PMDD Awareness UK and an awareness month in April. The new website is almost ready and I am looking for women who would like to share their story/write about a certain aspect of PMDD. There will be ideas on the website of how you can help raise more awareness of PMS and PMDD, and ways that you can contribute to the website. Email me direct at pmddawareness@live.com if you would like to contribute to the website..

Thank you to NAPS and Mr Nick Panay for letting me peep through the window into the medical world, and for supporting my work so far. I hope that one day I might be able to stand at the front of the room and share my story, to give GP's and students a real life account of what PMS/PMDD really feels like, from my own personal story and from the stories I have read of hundreds of other PMDD sufferers over the years. If you ever get a spare slot, give me a call!

By Cat Hawkins

Mother, Artist, Writer, PMS Lay Champion, PMDD Blogger, Facebook Support Group Owner
Founder of PMDD Awareness UK – A grass-roots organisation with a mission to change the way the UK views menstrual health problems. Promoting a positive menstrual outlook.

(All personal views expressed are my own.  An edited version of my report can be found in the NAPS February bulletin  www.pms.org)

Wednesday, 27 February 2013

Where I am with things now...

The following is part of a message I wrote to my new UK support group...  I thought I'd share here too.

When I started the support groups I was very active in all of them.  I was still struggling with my PMDD and needed the valuable words of support and advice that you can find in the group, however, life moves on and my struggles are far more under my control and I am beginning to focus my time on other things.  What this means is although I am the group owner, I may not be in here and posting all the time.  I will always respond to anything I'm tagged in, but I unfortunately don't have the time I used to have to dedicate to the groups.  There was one point in my life when my PMDD groups were the first thing I checked in the morning and the last thing at night!  I have always seen the need to create a UK group, so this, I think, will be the last group I set up!

I have been writing my blog for about 6 years and writing has my saviour so many times.  Go back a few years and you can read my posts from when I was at my worst, right up to now where I tend to focus my writing into creating more positive articles and blogs.  It has proved quite popular and I thank the Goddess for ever comment that keeps me writing.  I get lots of emails and inbox messages for people looking for help.  It would be impossible for me to help and support everyone, but what I can do is create a space where you can do it for each other.

I have lived with this since I was 13, and have tried many medications, birth controls, IUD's etc but the only thing that worked for me was changing the way I saw my period. I began working with the natural ups and downs.  I learned to deal better with stress and I make sure I avoid stressful situations.  Looking after myself, honouring what having a powerful connection to the cycle means has helped turn things around for me. I do not believe in medications.  I do not believe this incurable.  I see PMDD as a severe imbalance within the system, with many factors contributing to the overall list of symptoms.  It's a whole mix up of low serotonin, adrenal fatigue, excess hormones or lack of, sensitivity to the hormonal changes, not enough healthy food and exercise, lack of sleep, traumatic situations, childhood baggage, unhealthy relationships, being over worked, and negative though patterns etc etc... possibly mixed up with some depression and other health conditions you may have, and possibly brought on by some kind of reaction to hormonal medication, pregnancy, or underlying problem in the sex organs.

I now manage my PMDD and life so that I rarely suffer the severe symptoms.  I'm not free of it, but neither would I want to be.  PMDD makes me look at my life and the things I am doing.  It stops me from taking on more than I can handle.  It makes me streamline my friendships so that I only have people around me who I trust and who understand me.  It has led me to become strong and there is nothing better than PMDD to teach you how to 'not sweat the small stuff'.  I have achieved this through stopping all meds and birth control, getting lots of counseling, moving on from bad relationships and stressful friendships, and becoming more aware of my cycle.  I use spiritual views and ideas to get me through, concepts about the menstrual cycle that I connected with in a spiritual way.  It's made me be more honest and open with those around me.  It makes me ask for help when I need it. 

My menstrual cycle has become a source of inspiration for me and I no longer fear it.  I know the cycle.  I know MY cycle.  I rest when I need to, I work hard when I can.  I see my life, much like a circus act.  I'm the plate spinner.  I get one going, then my mood changes, so I set another one spinning... I keep going till there are things to do no matter what mood I'm in, so I focus on those things in turn as my mood changes.  Sometimes I drop all the plates, and after a rant, rest or cry, I start picking them back up and get spinning again.

 

One thing I have realised is that I will never be able to work a normal 9-5.  I cannot fit into the schedules of the outside world, so I will no longer strive to.  It has always been my plan to run my own business or go self employed, so that is now where I see myself heading.  One step at a time, always chipping away.  I used to think I would never get anywhere, locked into the crazy cycles, but now I see a path where before there was none.  

By meeting others and realising I was not alone I broke the first chain.  By learning from others and never giving up, never closing my mind to new possibilities I have got this far and so can you.  No matter what path you follow, whether it's meds, hormones, lifestyle, spirituality, alternative treatments or surgery, you will hopefully find someone else in the same boat who can relate, and who can offer support.  We should always be accepting of other peoples choices and remember that what may have worked for us may not work for someone else.  We can always offer a word of support even if we don't fully relate...

Currently, I am building a new website to launch PMDD Awareness UK.  I am hoping this will become a base for PMDD news and campaigns in the UK.  I am also hoping that women will join in in raising awareness, and the website will eventually provide posters to download, and info sheets to give to GP's.  I am also looking at creating a mood chart, downloadable from the website.  There are no organisations working solely for PMDD in the UK.  NAPS do a great job in working on behalf of women with PMDD, and I liase with them regarding PMDD Awareness issues.  They are still our only official organisation and a great place to get info and help.  They are also all set up for that kind of thing, so me, with my PMDD Awareness UK plans will need to continue to ask women to step forward, join the tribe and help try and change things.  You know that saying.. 'if you want something done...' well WE need something done about the state of PMDD and how it is dealt with, WE need to be prepared to write a letter or put up a poster...  It may only seem like small steps, but that's all we need to get started.  It's better than no steps at all! If you haven't liked the PMDD Awareness UK page, please come and do so www.facebook.com/pmddawarenessuk

Lots of love to you all! I wouldn't have got here if it hadn't been for these groups and the readers comments and messages on my blog! all of which have supported me along my journey, so thank you!


If you would like to join my new UK Facebook support group, and you currently live in the UK, please follow this link!  https://www.facebook.com/groups/ukpmddsupport/

Tuesday, 4 December 2012

Mind! here we come! and NEW NAPS FORUM!

After my third attempt at trying to get through to Mind, the mental health charity regarding the inclusion of PMDD on their website, I finally wrote again, making it quite clear I wasn't happy.  This time I got a reply.  I have to write a proposal form so it can be taken into consideration at the next meeting which is in February 2013.

I passed the information on to Jackie Howe from NAPS as I felt a little out of my depth.  I believe we are now going to be working on this together, as I saw this on their website today!

http://www.pms.org.uk/About+PMS/Bulletins/2012+Bulletins/November+2012/item1299/
Cat Hawkin’s has been working very hard to create greater awareness of severe PMS/PMDD and has been a major campaigner to gain acceptance by the WHO of PMMD in their International Classification of diseases. She has received notification that she can now make a proposal to MIND, the mental health charity, for a web page ,called Understanding PMDD.NAPS will be taking forward this proposal with Cat. Many women.... read more..
Feeling pretty good about this!  Let's hope we get the recognition we need.  The more people who learn about PMDD, the more the demand for research and development of better treatments.. which in turn leads to a better general understanding of PMDD and an easier journey to healing and management of symptoms.

In other news...

NAPS have re opened their forum!  It's free to join and was always a hive of conversation.  Pop on over there and sign up!  While you are there, take a look at their membership.  You can get access to specialists and advice.  NAPS is the only charity working for PMS and PMDD, every member helps them to do more work and raise more awareness...


Tuesday, 16 October 2012

28 Days Poster

The idea came to me last night...

Here is my 28 Days painting, with a little magic from Photoshop, turned into a spot the difference style poster!

This painting always makes me giggle, so it's nice to have found a use to share it more.

Come on over to Facebook to share from one of my pages...

www.facebook.com/meetmypmdd
www.facebook.com/pmddawarenessuk


(c) Cat Hawkins - www.chaoticat.com

Monday, 15 October 2012

PMDD Awareness UK

It's a new moon today, AND it's PMS AWARENESS WEEK so there is no better time to launch my new project. A place to keep all the campaign work separate to the blogging, and somewhere to focus all the PMDD Awareness stuff....

INTRODUCING.....

https://www.facebook.com/pages/PMDD-Awareness-UK/113398732150471

There will be a new website coming soon!

I will be continuing all the campaigning over there and hopefully we can get bigger and stronger in 2013.  I will of course still give updates here, but this new project will give me somewhere to focus more on raising awareness in the UK.

Please come and give me a like, even if you are not in the UK. By fighting for this here, I hope it will change things all around the world. ♥

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